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Paritaprevir, ritonavir, ombitasvir, and dasabuvir with and without ribavirin in people with HCV genotype 1 and recent injecting drug use or receiving opioid substitution therapy

Authors :
Amanda Erratt
Jordan J. Feld
Curtis Cooper
Gail V. Matthews
Sione Crawford
Adrian Dunlop
David R. Shaw
Catherine A.M. Stedman
Kathy Petoumenos
Tanya L. Applegate
Margaret Hellard
Phillipa Marks
Brian Conway
Erika Castro
Alberto Moriggia
Evan B Cunningham
Jeff Powis
Ian Kronborg
Gregory J. Dore
Patrick Schmid
Edward Gane
Christopher S. Fraser
Julie Bruneau
Olav Dalgard
Jean-Pierre Daulouède
Karine Lacombe
Jason Grebely
Philip Bruggmann
Behzad Hajarizadeh
Source :
International Journal of Drug Policy. 62:94-103
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Background: Direct-acting antiviral therapy for hepatitis C virus (HCV) infection is safe and effective, but there are little data among people who have recently injected drugs. This study evaluated the efficacy, and safety of paritaprevir/ritonavir, ombitasvir, dasabuvir with or without ribavirin for chronic HCV genotype (G) 1 among people with recent injecting drug use and/or receiving OST. Methods: D3FEAT is an international open-label study that recruited treatment-naive participants with recent injecting drug use (previous 6 months) and/or receiving OST with chronic HCV G1 infection between June 2016 and February 2017 in seven countries. Participants received paritaprevir/ritonavir, ombitasvir, dasabuvir with (G1a) or without ribavirin (G1b) administered twice daily in a one-week electronic blister pack (records timing of each dose) for 12 weeks. The primary endpoint was undetectable HCV RNA 12 weeks post-treatment (SVR12). Results: Among 87 participants (median age 48 years), 23% were female, 8% had cirrhosis, and 90% had G1a. Overall, 71% were receiving OST, 61% injected in the previous six months, 45% injected in the previous month, and 15% injected > daily. Treatment completion was 97% (84 of 87). There were no virological breakthroughs, but three discontinuations (loss to follow-up, n = 1; non-adherence, n = 1; incarceration, n = 1). SVR was 91% (79 of 87, 95% CI, 83%–96%). Five participants who completed treatment did not have SVR (loss to follow-up, n = 1; death, n = 1; virologic relapse, n = 3). Drug use prior to and during treatment did not impact SVR12. Treatment-related adverse events were observed in 46 (53%) patients (six grade 3, no grade 4). Five (6%) patients had at least one serious adverse event (two possibly/probably related to therapy; nausea and myoclonus). Two cases of reinfection were observed. Conclusion: Paritaprevir/ritonavir, ombitasvir, and dasabuvir with or without ribavirin for 12 weeks is effective among people with HCV genotype 1 with recent injecting drug use and/or receiving OST.

Details

ISSN :
09553959
Volume :
62
Database :
OpenAIRE
Journal :
International Journal of Drug Policy
Accession number :
edsair.doi.dedup.....91ed53cf823d3bc23d54c91273597287